File Download
There are no files associated with this item.
Links for fulltext
(May Require Subscription)
- Publisher Website: 10.3389/fpubh.2023.1185957
- Scopus: eid_2-s2.0-85169683111
- WOS: WOS:001058334200001
- Find via

Supplementary
- Citations:
- Appears in Collections:
Article: COVID-19 and cognitive performance: a Mendelian randomization study
| Title | COVID-19 and cognitive performance: a Mendelian randomization study |
|---|---|
| Authors | |
| Keywords | cognitive performance COVID-19 inflammatory markers Mendelian randomization SARS-CoV-2 infection |
| Issue Date | 22-Aug-2023 |
| Publisher | Frontiers Media |
| Citation | Frontiers in Public Health, 2023, v. 11 How to Cite? |
| Abstract | Background: A substantial proportion of individuals with COVID-19 experienced cognitive impairment after resolution of SARS-CoV-2 infection. We aimed to evaluate whether genetic liability to SARS-CoV-2 infection per se, or more severe COVID-19, is causally linked to cognitive deficit. Methods: We firstly performed univariable Mendelian randomization (MR) analysis to examine whether genetic liability to SARS-CoV-2 infection, hospitalized and severe COVID-19 is causally associated with cognitive performance. To dissect the causal pathway, multivariable MR (MVMR) analysis was conducted by adjusting for five inflammatory markers [C-reactive protein, interleukin (IL)-1β, IL-6, IL-8, and tumour necrosis factor α, as proxies of systemic inflammation]. Results: In univariable MR analysis, host genetic liability to SARS-CoV-2 infection was associated with lower cognitive performance [inverse variance weighted (IVW) analysis, estimate: −0.023; 95% Confidence Interval (CI): −0.038 to −0.009]. Such causal association was attenuated in MVMR analysis when we adjusted for the five correlated inflammatory markers in one analysis (IVW analysis, estimate: −0.022; 95% CI: −0.049 to 0.004). There was insufficient evidence of association for genetic liability to hospitalized and severe COVID-19 with cognitive performance. Conclusion: The causal effect of host genetic liability to SARS-CoV-2 infection on reduced cognitive performance may be mediated by systemic inflammation. Future studies examining whether anti-inflammatory agents could alleviate cognitive impairment in SARS-CoV-2-infected individuals are warranted. |
| Persistent Identifier | http://hdl.handle.net/10722/339292 |
| ISSN | 2023 Impact Factor: 3.0 2023 SCImago Journal Rankings: 0.895 |
| ISI Accession Number ID |
| DC Field | Value | Language |
|---|---|---|
| dc.contributor.author | Tang, Ching-Man | - |
| dc.contributor.author | Li, Gloria Hoi-Yee | - |
| dc.contributor.author | Cheung, Ching-Lung | - |
| dc.date.accessioned | 2024-03-11T10:35:28Z | - |
| dc.date.available | 2024-03-11T10:35:28Z | - |
| dc.date.issued | 2023-08-22 | - |
| dc.identifier.citation | Frontiers in Public Health, 2023, v. 11 | - |
| dc.identifier.issn | 2296-2565 | - |
| dc.identifier.uri | http://hdl.handle.net/10722/339292 | - |
| dc.description.abstract | <p><strong>Background:</strong> A substantial proportion of individuals with COVID-19 experienced cognitive impairment after resolution of SARS-CoV-2 infection. We aimed to evaluate whether genetic liability to SARS-CoV-2 infection <em>per se</em>, or more severe COVID-19, is causally linked to cognitive deficit.</p><p><strong>Methods:</strong> We firstly performed univariable Mendelian randomization (MR) analysis to examine whether genetic liability to SARS-CoV-2 infection, hospitalized and severe COVID-19 is causally associated with cognitive performance. To dissect the causal pathway, multivariable MR (MVMR) analysis was conducted by adjusting for five inflammatory markers [C-reactive protein, interleukin (IL)-1β, IL-6, IL-8, and tumour necrosis factor α, as proxies of systemic inflammation].</p><p><strong>Results:</strong> In univariable MR analysis, host genetic liability to SARS-CoV-2 infection was associated with lower cognitive performance [inverse variance weighted (IVW) analysis, estimate: −0.023; 95% Confidence Interval (CI): −0.038 to −0.009]. Such causal association was attenuated in MVMR analysis when we adjusted for the five correlated inflammatory markers in one analysis (IVW analysis, estimate: −0.022; 95% CI: −0.049 to 0.004). There was insufficient evidence of association for genetic liability to hospitalized and severe COVID-19 with cognitive performance.</p><p><strong>Conclusion:</strong> The causal effect of host genetic liability to SARS-CoV-2 infection on reduced cognitive performance may be mediated by systemic inflammation. Future studies examining whether anti-inflammatory agents could alleviate cognitive impairment in SARS-CoV-2-infected individuals are warranted.</p> | - |
| dc.language | eng | - |
| dc.publisher | Frontiers Media | - |
| dc.relation.ispartof | Frontiers in Public Health | - |
| dc.rights | This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License. | - |
| dc.subject | cognitive performance | - |
| dc.subject | COVID-19 | - |
| dc.subject | inflammatory markers | - |
| dc.subject | Mendelian randomization | - |
| dc.subject | SARS-CoV-2 infection | - |
| dc.title | COVID-19 and cognitive performance: a Mendelian randomization study | - |
| dc.type | Article | - |
| dc.identifier.doi | 10.3389/fpubh.2023.1185957 | - |
| dc.identifier.scopus | eid_2-s2.0-85169683111 | - |
| dc.identifier.volume | 11 | - |
| dc.identifier.eissn | 2296-2565 | - |
| dc.identifier.isi | WOS:001058334200001 | - |
| dc.identifier.issnl | 2296-2565 | - |
